Intravascular malignant lymphomatosis
Intravascular malignant lymphomatosis
复制标题
血管内恶性淋巴瘤病
DOI：
10.1007/s00234-002-0808-9
复制
发表时间：
2002
期刊：
影响因子：
2.8
通讯作者：
J. Chiras
中科院分区：
文献类型：
--
作者：
N. Martin;K. Mokhtari;A. Béhin;F. Lafitte;K. Hoang;J. Chiras
血管内恶性淋巴瘤病是一种罕见的，可能经常被忽视的疾病，其特征是大量的淋巴细胞血管内增殖，通常预后不良。CT和MRI表现无特异性;最有提示性的发现是不对称的、双侧的、T2加权的对比增强高信号区以及皮质和基底节的梗死样病变。我们报告了两个以前未报告的硬脑膜和脊髓受累的患者。
Intravascular malignant lymphomatosis is a rare and probably often overlooked disease characterised by massive intravascular proliferation of lymphoid cells, usually with a poor prognosis. CT and MRI appearances are nonspecific; the most suggestive finding being both asymmetrical, bilateral, contrast enhancing high-signal areas on T2 weighting and infarct-like lesions of the cortex and basal ganglia. We report two patients with previously unreported dural and spinal cord involvement.